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A Novel Strategy towards the Total Synthesis of Cyclopeptide Alkaloids

机译:一种完全合成环肽生物碱的新策略

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摘要

Since the first structural determination of pandamine (1) by Goutarel and Pai's in 1963, the family of cyclopeptide alkaloids has grown rapidly and now encompasses over 200 compounds. These 13-, 14-, and 15-membered macrocycjes typically contain a para- or metacyclophane unit with a characteristic aryl-alkyl ether linkage. The widespread occurence of these compounds in nature makes them an important class of natural products. However, little is known about their biological and pharmacological properties due to their limited availability, The development of a practical synthetic method is therefore of utmost importance.
机译:自从Goutarel和Pai's在1963年首次确定潘达明(1)的结构以来,环肽生物碱家族已迅速发展,现已涵盖200多种化合物。这些13元,14元和15元大环基通常包含具有特征性芳基-烷基醚键的对-或间环烷单元。这些化合物在自然界中的广泛存在使它们成为一类重要的天然产物。但是,由于它们的有限可用性,对其生物学和药理学性质知之甚少。因此,开发实用的合成方法至关重要。

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